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OpenTrials
Completed

NCT Number: NCT04219852

Contraception and Bariatric Surgery: Evaluation of Contraception and Contraceptive Knowledge of Women Undergoing Bariatric Surgery at the University Hospital of Reims

Obesity is a public health phenomenon affecting more than 17% of women in France, and more than 20% of men and women in Champagne-Ardenne.

Obese women are more likely to have an unplanned pregnancy, whereas these pregnancies are more at risk than women of normal weight and should be planned or considered after weight loss. These women are also often less well followed in terms of gynecology and especially on contraception.

More and more patients are opting for bariatric surgery. However, bariatric surgery is not trivial. Indeed, the important loss of weight expected is at risk of nutritional deficiencies. In addition, a large number of patients are still obese during the months following surgery. This is why pregnancy is theoretically contraindicated within 12 or 18 months postoperatively.

Women with bariatric surgery must have been properly informed of these risks so that they can choose a contraceptive method, and that can be adapted to both their risk factors and the surgical technique performed.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Observational

Primary location

Chu Reims

Reims, 51092, France

About this study

The purpose of this study is to describe contraception in obese women who have undergone bariatric surgery in Champagne-Ardenne.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women between 18 and 50 years old
  • Followed at Reims University Hospital after bariatric surgery
  • Pre-menopausal status
  • Accepting to participate in the study

Exclusion criteria

  • Women less than 18 or more than 50 years old
  • Women with postmenopausal status
  • Women refusing to participate

Treatment and study plan

Data Collection

Other

data collection

Primary outcomes

  1. contraception method

    Time frame: Day 0

    Presence of contraception during the postoperative 3 months consultation

Sponsors and collaborators

Lead sponsor

CHU de Reims

Other

Registry information

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jan 7, 2020
Registry last updated
Mar 3, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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